Roche Pharma Research and Early Development, Neuroscience and Rare Diseases, Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd., Grenzacherstrasse 124, 4070, Basel, Switzerland.
Neuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland.
BMC Neurosci. 2024 Mar 15;25(1):18. doi: 10.1186/s12868-024-00861-4.
Sensory processing in the auditory brainstem can be studied with auditory brainstem responses (ABRs) across species. There is, however, a limited understanding of ABRs as tools to assess the effect of pharmacological interventions. Therefore, we set out to understand how pharmacological agents that target key transmitter systems of the auditory brainstem circuitry affect ABRs in rats. Given previous studies, demonstrating that Nrxn1α KO Sprague Dawley rats show substantial auditory processing deficits and altered sensitivity to GABAergic modulators, we used both Nrxn1α KO and wild-type littermates in our study. First, we probed how different commonly used anesthetics (isoflurane, ketamine/xylazine, medetomidine) affect ABRs. In the next step, we assessed the effects of different pharmacological compounds (diazepam, gaboxadol, retigabine, nicotine, baclofen, and bitopertin) either under isoflurane or medetomidine anesthesia. We found that under our experimental conditions, ABRs are largely unaffected by diverse pharmacological modulation. Significant modulation was observed with (i) nicotine, affecting the late ABRs components at 90 dB stimulus intensity under isoflurane anesthesia in both genotypes and (ii) retigabine, showing a slight decrease in late ABRs deflections at 80 dB stimulus intensity, mainly in isoflurane anesthetized Nrxn1α KO rats. Our study suggests that ABRs in anesthetized rats are resistant to a wide range of pharmacological modulators, which has important implications for the applicability of ABRs to study auditory brainstem physiology.
听觉脑干中的感觉处理可以通过跨物种的听觉脑干反应(ABR)进行研究。然而,人们对 ABR 作为评估药物干预效果的工具的理解有限。因此,我们着手了解靶向听觉脑干电路关键递质系统的药物如何影响大鼠的 ABR。鉴于先前的研究表明,Nrxn1α KO Sprague Dawley 大鼠表现出明显的听觉处理缺陷和对 GABA 能调节剂的敏感性改变,我们在研究中同时使用了 Nrxn1α KO 和野生型同窝仔鼠。首先,我们探究了不同常用麻醉剂(异氟烷、氯胺酮/甲苯噻嗪、美托咪定)如何影响 ABR。在下一步中,我们评估了不同药理学化合物(地西泮、加巴喷丁、瑞替加滨、尼古丁、巴氯芬和比托特滨)在异氟烷或美托咪定麻醉下的作用。我们发现,在我们的实验条件下,ABR 受多种药理学调制的影响不大。在异氟烷麻醉下,在 90 dB 刺激强度下,尼古丁(i)显著调制了晚期 ABR 成分,在两种基因型中均如此;而在 80 dB 刺激强度下,瑞替加滨(ii)则轻微降低了晚期 ABR 偏转,主要是在异氟烷麻醉的 Nrxn1α KO 大鼠中。我们的研究表明,麻醉大鼠的 ABR 对广泛的药理学调节剂具有抗性,这对 ABR 应用于研究听觉脑干生理学具有重要意义。